1
Ozone oxidation of oleic acid surface films decreases aerosol CCN 1
activity 2
3 A. N. Schwier,1 N. Sareen,1 T. L. Lathem,2 A. Nenes, 2,3,* and V. F. McNeill1,* 4
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1Department of Chemical Engineering, Columbia University, New York, New York USA 6
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2School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, Georgia, 8
USA 9
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3School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, 11
Georgia USA 12
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*to whom correspondence should be addressed. 14
[email protected], [email protected] 15
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Abstract 24
Heterogeneous oxidation of aerosols composed of pure oleic acid (C18H34O2, an unsaturated fatty 25
acid commonly foundin continental and marine aerosol)by gas-phase O3 is known to increase 26
aerosol hygroscopicity and activity as Cloud Condensation Nuclei (CCN). Whether this trend is 27
preserved when the oleic acid is internally mixed with other electrolytes is unknown and 28
addressed in this study. We quantify the CCN activity of sodium salt aerosols (NaCl, Na2SO4) 29
internally mixed with sodium oleate (SO) and oleic acid (OA). We find that particles containing 30
roughly one monolayer of SO/OA show similar CCN activity to pure salt particles, whereas a 31
tenfold increase in organicconcentration slightly depresses CCN activity. O3 oxidation of these 32
multicomponent aerosols has little effect on the critical diameter for CCN activation for 33
unacidifiedparticles at all conditions studied, and the activation kinetics of the CCN are similar 34
in each case to those of pure salts.SO-containing particles which are acidified to atmospherically 35
relevant pH before analysis in order to form oleic acid, however, show depressed CCN activity 36
upon oxidation. This effect is more pronounced at higher organicconcentrations.The behavior 37
after oxidation is consistent with the disappearance of the organic surface film, supported by 38
Köhler Theory Analysis (KTA).κ-Köhler calculations show a small decrease in hygroscopicity 39
after oxidation.The important implication of this finding is that oxidative aging may not always 40
enhance the hygroscopicity of internally mixed inorganic-organic aerosols. 41
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3
1. Introduction 46
Surface-active molecules contain both hydrophilic and hydrophobic moieties;therefore, they tend 47
to partition at the gas-liquid interface of aqueous solutions. Given that both water and surface-48
active organics are ubiquitous in tropospheric aerosols,organic films have long been 49
hypothesizedto exist on aerosol surfaces[Ellison et al., 1999; Gill et al., 1983] with potentially 50
important consequences for atmospheric chemistry and climate. Organic films may affect the 51
ability of the aerosol to act as CCN[Andrews and Larson, 1993; Asa-Awuku et al., 2008; Chuang 52
et al., 1997; Ervens et al., 2005; Facchini et al., 1999; Novakov and Penner, 1993; Shulman et 53
al., 1996], ice nuclei[Cziczo et al., 2004; DeMott et al., 2003; Kärcher and Koop, 2005],and alter 54
aerosoloptical properties[Bond and Bergstrom, 2006; Dinar et al., 2008; Kanakidou et al., 2005; 55
Malm and Kreidenweis, 1997; Mircea et al., 2005]. These films may act as a barrier to mass 56
transport across the gas-liquid interface, with implications for aerosol heterogeneous 57
chemistry[Folkers et al., 2003; McNeill et al., 2006; Thornton and Abbatt, 2005] and the rate of 58
water uptake[Asa-Awuku et al., 2009; Cruz and Pandis, 2000; Demou et al., 2003; Garland et 59
al., 2005; Gill et al., 1983; Hemming and Seinfeld, 2001; Nenes et al., 2002; Rubel and Gentry, 60
1984; Rudich et al., 2000; Saxena and Hildemann, 1997]. Surface-active organics can impact 61
CCN activity by lowering aerosol surface tension, thus affecting the Kelvin term of the Köhler 62
equation[Shulman et al., 1996], but they can also affect the Raoult term by altering ns, the 63
number of moles of solute, especiallywhen surface-bulk partitioning of solute is taken into 64
account[Kokkola et al., 2006; Sorjamaa et al., 2004; Sorjamaa and Laaksonen, 2006]. 65
66
Oleic acid (C18H34O2), a surface-active monounsaturated long-chain fatty acid, has been detected 67
in urban, rural and marine aerosols[Cheng and Li, 2005; Graham et al., 2003; Kawamura et al., 68
4
2003; Limbeck and Puxbaum, 1999; Robinson et al., 2006; Schauer et al., 1996, 2002; Simoneit 69
et al., 2004; Stephanou and Stratigakis, 1993; Yue and Fraser, 2004]. It is the most common 70
fatty acid found in plant membranes, is prevalent in many cooking oils, and it is used as a marker 71
for meat cooking aerosols[Rogge et al., 1991].Ozonolysis of oleic acid yields nonanal, nonanoic 72
acid, 9-oxononanoic acid, and azelaic acid under humid conditions, and high molecular weight 73
products under dry conditions[Hearn et al., 2005; Hearn and Smith, 2004; Katrib et al., 2005a; 74
McNeill et al., 2007; Rudich et al., 2007; Smith et al., 2002; Thornberry and Abbatt, 2004; Vesna 75
et al., 2008, 2009; Zahardis et al., 2005, 2006a; Zahardis and Petrucci, 2007].Under 76
atmospherically-relevant conditions, nonanal primarily partitions to the gas phase, while the 77
other products remain in the condensed phase. Dueto the importance of oleic acid as a 78
tracerspecies[Rogge et al., 1991] and its relatively well-understood O3 oxidation mechanism, 79
many studies of the kinetics of oleicacid oxidation have been performed on systems of varying 80
morphology, including pure oleic acid particles[Broekhuizen et al., 2004b; Hearn et al., 2005; 81
Hearn and Smith, 2004; Hung et al., 2005; Katrib et al., 2005a; Lee and Chan, 2007; Morris et 82
al., 2002; Pfrang et al., 2010; Reynolds et al., 2006; Sage et al., 2009; Smith et al., 2002; Vesna 83
et al., 2008; Zahardis et al., 2005, 2006a, 2006b; Ziemann, 2005], mixed organic particles[Hearn 84
and Smith, 2005; Hung and Ariya, 2007; Nash et al., 2005], films on polystyrene beads[Katrib et 85
al., 2004, 2005b], films on aqueous sea salt aerosol[King et al., 2004], films in coated wall flow 86
tube studies[de Gouw and Lovejoy, 1998; Knopf et al., 2005; Moise and Rudich, 2000, 2002; 87
Thornberry and Abbatt, 2004], and films on crystal surfaces[Asad et al., 2004]. 88
89
Pure organic aerosols are generally less hygroscopic and CCN active than deliquescent inorganic 90
particles (such as NaCl or (NH4)2SO4)[Petters and Kreidenweis, 2007]. Oxidation of organic 91
5
aerosol material can increase the number of polar, hydrophilic functional groups present in the 92
condensed phase, potentially leading to increased hygroscopicity and CCN activity. Oleic acid 93
particles have been used extensively as a model system to study the effect of oxidation on the 94
CCN activity of organic particles.Kumar et al.[2003] created pure oleic acid particles through 95
homogenous nucleation and observed no activation for particle sizes up to 140 nm and ≤ 0.6% 96
supersaturation (SS). Abbatt et al.[2005] studied the CCN activity of ammonium sulfate aerosols 97
coated with oleic acid and found that particles with thin (~2.5-5 nm) coatings of oleic acid were 98
not CCN active, but that CCN activity increased when the organic mole fraction increased. This 99
somewhat counterintuitive result was attributed to the fact that the particle diameter increased 100
with increasing organic mass fraction, reducing the magnitude of the Kelvin effect.Broekhuizen 101
et al.[2004a] found that oxidation products of oleic acid(nonanoic acid and azelaic acid) were 102
highly CCN active. In a separate study, they found that CCN activity was enhanced after 103
oxidation for both pure oleic acid particles and particles formed by atomizing a solution of oleic 104
acid in methanol[Broekhuizen et al., 2004b]. The enhancement in CCN activity occurred at very 105
high ozone exposures (~0.4 atms) for pure oleic acid particles, and at atmospherically relevant 106
exposures (<1x10-4atms) for the oleic acid/methanol particles.Shilling et al.[2007] determined 107
that 200 nm mobility diameter oleic acid particles, generated through either homogenous 108
nucleation or atomization, became CCN active at 0.66(±0.06)%supersaturation after exposure to 109
greater than 0.01 atmsO3. 110
111
Despite its atmospheric relevance, the response of mixed inorganic/oleic acid particles to 112
oxidation has not been considered in published CCN activity studies. This is an important 113
omission, because the acid almost always coexists in the atmosphere with inorganic salts. Little 114
6
is known about the interactions of oleic acid and its oxidation products with water in a high ionic 115
strength environment. These issues are addressed in this study. An aerosol flow tube reactor 116
coupled with a continuous flowcloud condensation nucleus counter is used to examine the effect 117
of ozone oxidation on the CCN activity of aerosol particles containing mixtures of sodium oleate 118
(SO)/oleic acid (OA) with inorganic salts (NaCl or Na2SO4). 119
2. Methods 120
2.1. Experimental.Sodium oleate (C18H33O2- .Na+), the sodium salt of oleic acid (C18H34O2), has 121
much higher solubility in water than oleic acid. It was used in these experiments to simplify the 122
preparation of aerosols containing a small, controlled amount of organic material. When the pH 123
of aerosols containing SO is lowered to atmospherically relevant values via acidification (see 124
details below), the oleateion converts to oleic acid according to: 125
C18H33O2- .Na+ + H3O+ ↔ C18H34O2 + H2O + Na+ (1) 126
127
For the experiments performed, the setup is shown in Figure 1. Polydisperse submicron aerosols 128
were generated using a constant output atomizer (TSI 3076). Atomizer solutions were prepared 129
using Millipore water with 0.001 M or 0.01 M SO (Sigma Aldrich) and 0.05 M NaCl. This 130
technique, using 0.001 M SO, was used by McNeill et al.[2007]to generate aerosols with an 131
inferred population-averaged oleate surface coverage of ~92%. The atomizer output was 132
combined with a humidified N2 dilution stream. This combined stream was sent through an 133
aerosol flow tube reactor (7.5 cm ID, 55 cm length). Relative humidity was measured at the 134
outlet of the flow tube reactor using a commercial hygrometer (Vaisala) and was maintained 135
between 62-67%. Ozone was generated by flowing O2 in an N2 carrier stream through a 136
7
photoreactor containing a Hg lamp (Jelight, Inc.). This stream entered the flow tube reactor 137
through a moveable stainless steel injector tube. Ozone concentrations of 0.2and1 ppm were 138
used. Total flow through the reactor was 0.8 LPM, with a reaction time of 3minutes.Processed 139
aerosols in the reactor effluent flowed through a diffusion drier before being characterized by a 140
Differential Mobility Analyzer (DMA, TSI 3080), a Condensation Particle Counter (CPC, TSI 141
3775) and a Continuous Flow Streamwise Thermal Gradient CCNChamber (CFSTGC, Droplet 142
Measurement Technologies)[Lance et al., 2006; Roberts and Nenes, 2005]. Aerosols were size-143
selected using the DMA, and the DMA output flow was split between the CPC and the CFSTGC. 144
0.8 LPM entered the DMA and split 0.5 LPM to the CFSTGC, 0.3 LPM to the CPC. Scanning 145
Mobility CCN Analysis[Moore et al., 2010] was used to determine the size-resolved CCN 146
activity of the aerosol, where the voltage applied to the DMA is scanned so that a complete 147
activation curve (fraction of classified particles acting as CCN) is obtained every 2 minutes. The 148
average total aerosol number concentration in the reactor output was 9.6 ± 2.0x104cm-3. The size 149
distribution of NaCl particles had a geometric surface area-weighted mean particle diameter of 150
202 ± 7nm with a geometric standard deviation of 1.59. Na2SO4 particles had a particle diameter 151
of 194 ± 5 nm with a geometric standard deviation of 1.63. 152
153
A second series of experiments was performed in order to test the sensitivity of CCN activity in 154
the mixed inorganic-SO aerosols to particle pH because atmospheric aerosols are typically 155
acidic[Keene et al., 2004; Zhang et al., 2007]. Under acidic conditions oleateexists in its un-156
ionized, lower-solubility form, oleic acid, according to Reaction 1. The atomizer output was 157
passed over an H2SO4 reservoir before combining with humidified N2 and entering the flow tube 158
reactor. Assuming an uptake coefficient γ=0.5[ten Brink, 1998], an aerosol surface area of Sa=6.2 159
8
±1.4x10-5 cm2cm-3, geometric volume-weighted mean diameter Dp=232 nm, and a residence time 160
of ~0.8 s in the H2SO4 reservoir, we estimate that the particles are acidified from an initial pH=8 161
to pH~0.4.The calculation methodology is shown in the supplementary material. Giventhat 162
thepKa of oleic acid = 5.02 [Riddick et al., 1986] and pH = 0.4, the ratio of oleate to non-163
dissociated oleic acid in the particles ([C18H33O2-]/[C18H34O2]) = 2.3988 x10-5, that is,nearly all 164
of the organic will be present as oleic acid under these conditions.For the acidification 165
experiments the total aerosol number concentration was 9.9 ± 1.4 x104 cm-3. 166
167
The following control experiments were also performed: “pure” sodium oleate particles were 168
generated by atomizing an aqueous solution of 0.001 M SO. In order to investigate possible 169
variations in pH buffering by differentcounterions,experiments were also performed using 170
aerosols atomized from solutions containing 0.001 M or 0.01 M SO and 0.06 M Na2SO4.Finally, 171
pure inorganic aerosols prepared from solutions containing 0.05 M NaClor 0.06 M Na2SO4 were 172
oxidized with 1 ppm O3 in the flow tube reactor, showing no significant deviation in CCN 173
activity from the pure salt calibrations without oxidation. 174
175
2.2 Data Analysis. Köhler Theory provides the framework used to describe cloud droplet 176
formation from activation of soluble particles [Cruz and Pandis, 1997; Gerber et al., 1977; Katz 177
and Kocmond, 1973]. A single-parameter expression of Köhler theory, referred to asκ-Köhler 178
theory, was introduced by Petters and Kreidenweis[2007]to account for the effect of variations in 179
solute hygroscopicity on CCN activity. Values of the hygroscopicity factor, κ, of 0.5<κ<1.4 are 180
typical for inorganic particles in the atmosphere. For hygroscopic organic particles, 0.01<κ<0.5, 181
9
whereas for non-hygroscopic materials (including highly hydrophobic organics)κapproaches 182
zero.κis derived from the CCN activity data as follows[Petters and Kreidenweis, 2007], 183
184
185
186
Here, dd is the critical dry activation diameter of the particle[m] (determined from CCN 187
activation experiments), Sis the water saturation ratio (S= 1 + 0.01Sc, where Sc is critical 188
supersaturation[%]), σs/a is the surface tension of water at the surface/air interface at the median 189
temperature of the CFSTGCcolumn, Mw is the molecular weight of water, R is the universal gas 190
constant, T isthe mediantemperature of the CFSTGCcolumn [K], and ρw is the density of water. 191
192
Köhler Theory Analysis (KTA) was also used to infer the surface tension of the mixed aerosol 193
before and after oxidation[Padro et al., 2007]. The following equations were used[Padro et al., 194
2007]: 195
2 33 2
/
(4)256 127
o o o
o w is a i i
w i
M
MRT M
ε υρ ρσ ω ε υ
ρ−
=⎛ ⎞ ⎛ ⎞ −⎜ ⎟ ⎜ ⎟
⎝ ⎠⎝ ⎠
196
where (5)
i
ii
i o
i o
m
m mρε
ρ ρ
=+
197
Here, Mo, Mi,ρoand ρirefer to the average molecular weight and density of the organic and 198
inorganic components of the aerosol, while υo andυi are effective van’t Hoff factors,εoandεiare 199
volume fractions, and mo, mi are the mass fractions of the organic and inorganic components, 200
3
3 2
4κ (2)27 lnd
Ad S
=
/4where (3)s a w
w
MARTσ
ρ=
10
respectively. The fitted CCN activity factor, ω, is determined from the log-log plots of 201
Scversusdd, fit to the equation[Asa-Awuku et al., 2010], 202
3/ 2 (6)c dS dω −= 203
κandω are related by 213 )27/4( κω A= . 204
3. Results 205
The results of our CFSTGC measurements for the SO/OA/NaCl and SO/OA/Na2SO4 systems are 206
shown in Figures 2-5. A complete list of calculated κ values (derived from eqs. (2) and (3)) and 207
power law exponents for the CCN activity data is available in the supplementary material. 208
209
3.1 SO/NaCl. As expected, pure SO/H2O aerosols are much less CCN active than NaCl aerosols 210
(Figure S1), withκ= 0.12 ± 0.004. As shown in Figures 2a and S1, the CCN activity of mixed 211
SO/NaCl particles generated from 0.001 M SO/0.05 M NaCl solutions (κ= 1.19 ± 0.03) is similar 212
to that of pure NaCl particles. The mixed particles with higher SOcontent show intermediate 213
CCN activity(κ= 0.87 ± 0.06) compared to particles with lower SO content and pure SO/H2O 214
particles. The mixed SO/NaCl aerosols exhibit similar wet activated diameter profiles to NaCl 215
particles (Figure 2b), indicating that the presence of oleate does not retard the activation kinetics 216
of the aerosol on the timescale of the CCN measurements[Engelhart et al., 2008; Moore et al., 217
2008]. Furthermore, for all these systems the critical supersaturation shows a power law 218
dependence of Sc ~ dd-1.42±0.04, suggesting that the CCN activity of these particles is described 219
fairly well by Köhler theory, with no significant solubility limitations or size-dependent surface-220
bulk partitioning effects. For a system that is perfectly described by Köhler Theory, we expect 221
the relationship to follow Sc ~ dd-1.5, as shown in eq. (6)[Padro et al., 2007]. 222
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223
CCN activity did not significantly change upon exposure to O3 for theunacidifiedmixed SO/NaCl 224
aerosols studied. Critical dry diameters changedby ~0.5% for the particles generated from 0.001 225
M SO/0.05 M NaCl solutions and ~1.6% for the particles generated from 0.01 M SO/0.05 M 226
NaCl solutions (Figure 2a); this leads to a changeof particle critical supersaturation by ~1% for 227
the former and ~3% for the latter. The change in CCN activity due to oxidation effectively falls 228
within the standard deviation of the non-oxidized data, showing relatively little effect of 229
oxidation to unacidifiedmixed SO/NaCl particles. Calculatedκvalues after oxidation for all 230
SO/NaCl aerosols were similar to the κ values prior to oxidation;κ=1.14 ± 0.02 for 0.001 M 231
SO/0.05 M NaCl and κ=0.83 ± 0.04 for 0.01 M SO/0.05 M NaCl. The change in CCN activity 232
wasnot dependent on the concentration of ozone used within the range studied here (0.2 – 1 233
ppm). The wet diameter profiles after oxidation are nearly identical to the non-oxidized SO/NaCl 234
particle wet diameters. This suggests that surface films, if present, do not retard CCN activation 235
kinetics and growth. 236
237
3.2 SO/Na2SO4. Because oleate oxidation generates organic acid products, it is possible that the 238
particle pH changes during oxidation, with implications forfatty acid solubility[Cistola et al., 239
1988]. In the unacidifiedSO/NaCl system, the formation of organic acidoxidation products may 240
result in the formation, and possible subsequent volatilization, of HCl, due to its high vapor 241
pressure. The net pH change is expected to differ in the SO/Na2SO4 system. The CCN activity 242
data for the SO/Na2SO4 experiments are shown in Figure 3. 243
244
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The CCN activity of the SO/Na2SO4 particles follows trends similar to what we observed for the 245
SO/NaCl particles. The CCN activity of the particles generated from 0.001 M SO/0.06 M 246
Na2SO4 solutions(κ= 0.71 ± 0.04) and 0.01 M SO/0.06 M Na2SO4 solutions (κ= 0.68 ± 0.03) is 247
roughly similar to that of pure Na2SO4 particles. The CCN activity changes littleupon oxidation, 248
and the resulting hygroscopic parameters (κ= 0.71± 0.02 and κ= 0.67 ± 0.03, respectively) are 249
similar to the non-oxidized SO/Na2SO4 particles, analogous to our observations for the 250
SO/NaClsystem. The wet diameter profiles are again very similar both before and after 251
oxidation, suggesting that there is no kinetic limitation to water uptake. 252
253
3.3 Acidified experiments: OA/NaCland Na2SO4. As an additional test of the effect of pH on 254
our observations of CCN activity for the SO/NaCl and SO/Na2SO4 systems, we performed a set 255
of experiments in which the atomized mixed particles were exposed to gas-phase H2SO4 before 256
oxidation. The goal of these experiments was to create a particle with a low pH typical of that of 257
atmospheric aerosols, conditions under which sodium oleate and the organic acid oxidation 258
products are in their un-ionized, lower-solubility forms (cf. Reaction (1)). As demonstrated in 259
Section 2, nearly all of the SO will be present as oleic acid under these conditions.The results of 260
these experiments are shown in Figure 4 and 5. 261
262
The CCN activity of acidified 0.001 M SO/0.05 M NaCl (κ= 1.14 ± 0.05) and 0.01 M SO/0.05 M 263
NaCl (κ= 0.97 ± 0.08) decreased after oxidation (κ= 1.07 ± 0.05 and 0.79 ± 0.02, respectively), 264
more noticeably at higher instrument supersaturations and SO concentrations (Figure 4 and 265
inset). The wet activated diameters do not show any kinetic limitations to water uptake. 266
13
Similarly, the acidified SO/Na2SO4 data shows similar CCN activity behavior to the acidified 267
SO/NaCl particles (Figure 5). The hygroscopicity values for both 0.001 M and 0.01 M SO/0.06 268
M Na2SO4 decrease after oxidation, and both follow the power law dependence expected from 269
Köhler theory (where Sc ~ dd-1.46±0.005 and Sc ~ dd
-1.37±0.002, respectively). 270
271
3.4 Köhler Theory Analysis.The parameters and results of the KTA calculations can be seen in 272
Tables 1-3. The initial in-particle concentrations of oleate and the inorganic salt were calculated 273
followingMcNeill et al.[2007]. After oxidation, we assume the oleate is completely oxidized to 274
form nonanal and azelaic, nonanoic, and 9-oxononanoic acids. The product yields reported 275
byVesna et al.[2009] were used. The density of 9-oxononanoic acid is unknown and was 276
assumed to be 1 g cm-3. The inorganic effective van’t Hoff parameter (υi), T, the fitted CCN 277
activity factor (ω), and ρw all varied with varying Sc and dd.To account for dissociation of the 278
organics, υo = 1 and 2 were tested, but the results for both salts at varying ozone concentrations, 279
regardless of the υo used,were the same to within 3%; the data for υo = 2 is shown. 280
281
The results suggest that the surface tension of the aerosols increases slightly after oxidation, 282
which is consistent with the breakup of the oleate monolayer (we have measured the surface 283
tension of bulk solutions saturated in NaCl and SOusing pendant drop tensiometry to be 44.4 ± 284
0.8dyn cm-1).The calculated surface tension values after oxidationfall between 64-75dyn cm-1, 285
slightly less thanthe surface tension of saturated NaCl and Na2SO4 solutions[Washburn, 286
2003].Vesna et al.[2009] found thata large portion of the aerosol organic mass after oleic acid 287
oxidation consisted of unidentified products (UP). Including these products inour KTA 288
14
calculations (assuming an average molar mass of 500 g mol-1anddensity of 1.4 g cm-3,[Turpin 289
and Lim, 2001]), gave very similar surface tension results compared to when only the 4 main 290
oxidation species are considered. Therefore, the single-phase approximationrepresents our 291
system well. 292
293
4. Discussion 294
The particles generated using 0.001 M SOatomizer solutions were designed such that the 295
particles with the surface-area weighted average diameter would be covered with approximately 296
1 monolayer of oleate/OA at 65% RH. Following McNeill et al.[2006], we estimated the 297
organicfractional coverage of the total available surface area of our aerosol population by, 298
(7)i i
i
ii
N
N
θΘ =
∑∑
299
whereθiand Ni are the fractional surface coverage of the aerosol and the number density in the 300
DMA size bin i,and Θis the overall fractional surface coverage. Assuming three things: that all 301
the organic partitions to the surface until saturated coverage is reached,that it is equally 302
distributed across the aerosol population in constant proportion to either NaCl or Na2SO4, and an 303
oleatefootprint of 48 Å2[Langmuir, 1917], we find that for the particles generated using 0.001 M 304
SO/0.05 M NaCl or 0.001 M SO/0.06 M Na2SO4 atomizer solutions, Θ≈0.83 (83% overall 305
surface coverage) and Θ≈1.01 (100%), respectively. This calculation also implies that smaller 306
particleswith larger surfacearea-to-volume ratios will not contain enough oleate for full 307
monolayer coverage, while thelarger particles will have complete monolayer coverage.There is 308
indirect evidence of monolayer formation at similar conditions from N2O5 uptake experiments by 309
15
McNeill et al.[2007]. In addition, McNeill et al.[2007] analyzed SO/NaCl particles formed using 310
this techniqueby SEM-EDAX,which showed the existence of uniform coatings of SO on the 311
particles.Using kinetic data fromMcNeill et al.[2007], we calculate the extent of oxidation in 312
particles with lower SO content to be76-100%, varying with O3 concentration. The reacto-313
diffusive length in the OA-O3 system is ~20 nm, so for particles with higher SO content, the 314
kinetic model of Smith et al. [2002], for reactions occurring in a near-surface layer of a pure 315
oleic acid particle, can be applied. Using their kinetic model and parameters, we calculate ~100% 316
oxidation. 317
Several studies on bulk systems have shown that when an oleic acid monolayer at the air-318
aqueous interface is exposed to ozone, the organic film breaks down, as evidenced by a decrease 319
in surface pressure[González-Labrada et al., 2006, 2007], disappearance of the vibrational sum 320
frequency generation signal [Voss et al., 2006, 2007], or neutron reflection[King et al., 2009]. 321
From these studies, it appears that the oxidation products leave the gas-particle interface soon 322
after oxidation. Nonanoic acid, 9-oxononanoic acid, and azelaic acid are more soluble in water 323
than oleic acid, and they may partition into the aqueous solution after they are formed. However, 324
there is evidence that azelaic acid[Tuckermann, 2007; Tuckermann and Cammenga, 2004] and 325
nonanoic acid[Caetano et al., 2007; Gilman et al., 2004; King et al., 2009] are surface-active and 326
CCN active[Broekhuizen et al., 2004a].McNeill et al.[2007]observed that nonanoic acid in wet 327
NaCl aerosols, in the absence of other oleic acid oxidation products, was volatile at room 328
temperature.Nonanal has been reported to enter the gas phase after it is formed[Katrib et al., 329
2004; Moise and Rudich, 2002; Thornberry and Abbatt, 2004; Voss et al., 2006; Wadia et al., 330
2000].Hung and Ariya[2007] analyzed the oxidation of mixed OA/NaCl particles using ATR-331
FTIR, and showedthat before oxidation, while increasing RH, there was no increase in the water 332
16
content of the particles, but after oxidation, there was an initial increase, then decrease in the 333
liquid water content. They determined that the hygroscopicity of OA/NaCl particles changed 334
after oxidation, but could vary and was affected by relative humidity levels. King et al.[2009] 335
used neutron scattering and surface pressure measurements to study the disappearance of an oleic 336
acid surface film on an aqueous subphase upon exposure to O3. They observed that roughly half 337
of the oxidation products remained at the surface, while the remainder were either released into 338
the gas phase or incorporated into the bulk. Consistent with our observations that CCN activity 339
was not enhanced compared to the pure salt for the particles generated using 0.001 M SO/0.05 M 340
NaCl or 0.001 M SO/0.06 M Na2SO4 atomizer solutions,they calculated, using Köhler theory, 341
that one monolayer of oleic acid on a 100 nm radius particle would not depress surface tension 342
during cloud droplet formation enough to affect the critical supersaturation point of the droplet. 343
Based on the assumption that the oleic acid oxidation would be complete and would lead to a 344
surface film of nonanoic acid, with azelaic acid dissolving into the bulk phase, they predicted 345
that the oxidation of an oleic acid surface film on an aerosol particle would decrease the critical 346
supersaturation required for droplet formation, increasing CCN activity. Surface-bulk 347
partitioning was not taken into account in that calculation[Kokkola et al., 2006; Sorjamaa et al., 348
2004; Sorjamaa and Laaksonen, 2006]. 349
350
Our KTA calculations show support for a smallincrease in particle surface tension upon 351
oxidation. Such an increase in surface tension could occur with the disappearance of a surfactant 352
film at the interface. However,our observation that the mixed inorganic/organic particles become 353
more organic-like in their CCN activity after oxidation is not inconsistent with the oxidation 354
products remaining at the interface.The high salt content of the particles prior to activation and 355
17
the acidic conditions would decrease the solubility of the oxidation products in these aerosols as 356
compared to the bulk films studied by other groups, possibly leading to phase separation. If 357
oxidation of an oleate surface layer is complete, it would result in the doubling of the number of 358
organic molecules present at the interface. In the absence of external pressure, oleate forms 359
expanded-state monolayers on aqueous surfaces, that is, the surface layer formed by the 360
hydrophobic tail groups is not well-ordered[Rideal, 1925; Schofield and Rideal, 1926]. 361
Immediately after forming, the oxidation products exist in a disordered double layer until they 362
dissolve into the bulk or are released into the gas phase, or sufficient water is taken up by the 363
particle to dissolve them. Transport to and self-assembly of surfactant products at the interface 364
may be slow after oxidation, occurring on timescales much longer than the residence time in our 365
experimental system[Lass et al., 2010; McIntire et al., 2010]. The work of McIntire et 366
al.[2010]on the ozonolysis of alkene self-assembled monolayers (SAMs) with internal double 367
bonds provides support for the formation of a complex, low-hygroscopicity organic surface layer 368
upon ozonolysis. They reported that ozonolysis did not increase the hygroscopicity of surface-369
bound alkenes, and it was hypothesized that the polar head groups of the oxidation products were 370
buried in a mixed organic layer after oxidation rather than at the air-organic interface. They 371
concluded that the three-dimensional structure of particles was critical for predicting aerosol 372
hygroscopicity and CCN activity. 373
374
For internal mixtures, κ can be described by a weighted linear sum of the components in the 375
system [Petters and Kreidenweis, 2007]. κ of azelaic acid was found to be ~0.1, while κ of the 376
other oxidation products is unknown. If we assume that κ for all oxidation products is 0.1 and 377
use the weighted sum approach, we find that the theoretical κ values after oxidation from 0.001 378
18
M SO/0.05 M NaCl and 0.001 M SO/0.06 M Na2SO4are 1.23 and 0.83, respectively.Possible 379
sources of error include the assumption of one κ value for the four main oxidation products. The 380
small difference between these theoretical κ valuesand our observations (κ= 1.19 and 0.71, 381
respectively) suggests that these particles can be accurately described as internally well-mixed. 382
383
Since most of the expected oleateozonolysis products are organic acids, a change in aerosol pH is 384
possible upon oxidation in the unacidified particles. Due to the possible formation of sodium 385
salts as well as organic acids, this maximum pH change assumes that only the three soluble 386
organic acid oleate oxidation products are formed and dissolve in the aqueous phase.Using the 387
pKa of each acid (azelaic acid (pKa=4.55), nonanoic acid (4.95), 9-oxononanoic acid (assumed 388
to be 4.95)), we can estimate the concentration of [H+] in our system after oxidation. The 389
calculation methodology is shown in the supplementary material. Assuming pH = 8 initiallyand 390
using product yields fromVesna et al.[2009], after complete oxidation of an aerosol with in-391
particle oleate concentration of 0.176 M[McNeill et al., 2007], the particles would have [H+] = 392
1.38mM, resulting in a final pH of ~3. This pH change is expected to be less in the SO/Na2SO4 393
system due to buffering by SO4-2, and negligible in the acidified particles. Fatty acid solubility 394
increases with increasing pH (basic conditions), complementing our observation that CCN 395
activity decreases upon oxidation for acidifiedparticles but shows little change for unacidified 396
particles.This highlights the importance of using atmospherically relevant pH in laboratory 397
studies involving fatty acid surface-bulk partitioning in aerosols.The activated droplet diameters 398
of the studied systems did not change after oxidation; this suggests that if there are any kinetic 399
barriers to hygroscopic growth in these systems, they may be due to the finite dissolution 400
timescale and not a water uptake barrier from the action of the organic surface layer. 401
19
5. Conclusions 402
We examined the effect of ozone oxidation on the CCN activity of aerosol particles containing 403
mixtures of sodium oleate (SO)/oleic acid (OA) with inorganic salts (NaCl or Na2SO4).Exposure 404
to O3led to decreased CCN activity for particles at atmospherically relevant pH. Wet (activation) 405
diameters of these particles were not significantly different frominorganic calibration standards, 406
suggesting that the activation kinetics are not affected by organic surface films. KTA indicatesa 407
slight increase in particle surface tension uponoxidation, consistent with breakup of the organic 408
film after oxidation.The κ values were calculated here for a reaction timescale of up to 3 minutes, 409
and might not accurately represent the real water uptake properties of an aged atmospheric 410
particle.We find that oxidative aging of mixed inorganic-organic aerosols may negatively affect 411
their hygroscopicity and CCN ability. 412
Acknowledgements 413
This work was funded by the NASA Tropospheric Chemistry program (grant NNX09AF26G) 414
and the ACS Petroleum Research Fund (grant 48788-DN14). AN acknowledges support from a 415
NSF CAREER grant, and TLL acknowledges support from a NSF Graduate Student Fellowship 416
and a GT Institutional Fellowship. 417
418
419
420
20
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30
782
Figure Captions 783
784 Figure 1.Experimental setup. The solutions were atomized, and combined with humidified N2; 785
this flow entered the flow tube reactor simultaneously with O3 in an N2 stream. The reactor 786
effluent passed through a drier before being characterized with a Differential Mobility Analyzer 787
(DMA), Condensation Particle Counter (CPC) and a Continuous Flow Streamwise Thermal 788
Gradient CCN Chamber (CFSTGC). 789
Figure 2.CCN activity of SO/NaCl particles. Particles generated from solutions containing 0.001 790
M or 0.01 M SO mixed with 0.05 M NaCl were exposed to O3 concentrations ranging between 791
0.2-1ppm in an aerosol flow tube reactor. Instrument supersaturation is shown as a function of 792
A) critical dry diameter and B) activated wet diameter. In both plots, the red dots represent the 793
salt calibration, and the red lines are guides to the eye. In panel A) an inset focuses on higher 794
supersaturations. In panel B) the gray lines indicate the standard deviation in the salt calibration. 795
Figure 3.CCN activity of SO/Na2SO4 particles. Particles generated from solutions containing 796
0.001 M or 0.01 M SO mixed with 0.06 M Na2SO4, were oxidized with 1 ppm O3 in an aerosol 797
flow tube reactor. Instrument supersaturation is shown as a function of A) critical dry diameter 798
and B) activated wet diameter. In both plots, the red dots represent the salt calibration, and the 799
red lines are guides to the eye. In panel A) an inset focuses on higher supersaturations. In panel 800
B) the gray lines indicate the standard deviation in the salt calibration. 801
Figure 4. CCN activity of SO/NaCl particles exposed to H2SO4. Particles generated from 802
solutions containing 0.001 M or 0.01 M SO mixed with 0.05 M NaCl were oxidized with 1 ppm 803
O3 in a flow tube reactor. Instrument supersaturation is shown as a function of A) critical dry 804
diameter and B) activated wet diameter. In both plots, the red dots represent the salt calibration, 805
and the red lines are guides to the eye. In panel A) an inset focuses on higher supersaturations. In 806
panel B) the gray lines indicate the standard deviation in the salt calibration. 807
Figure 5. CCN activity of SO/Na2SO4 particles exposed to H2SO4. Particles generated from 808
solutions containing 0.001 M or 0.01 M SO mixed with 0.06 M Na2SO4 were oxidized with 1 809
ppm O3 in a flow tube reactor. Instrument supersaturation is shown as a function of A) critical 810
dry diameter and B) activated wet diameter. In both plots, the red dots represent the salt 811
calibration, and the red lines are guides to the eye. In panel A) an inset focuses on higher 812
supersaturations. In panel B) the gray lines indicate the standard deviation in the salt calibration. 813
Tables 814
815
Table 1. KTA Parameters used before and after oxidation, based on in-particle concentrations of 816
0.176 or 1.76 M oleate and either 8.6 M NaCl or 10.6 M Na2SO4 . 817 818
31
0.176 M 1.76 M KTA
Parameters
Before Oxidation
After Oxidation
(0.2-1ppm)
Before Oxidation
After Oxidation
(1ppm) NaCl Na2SO4 NaCl Na2SO4 NaCl Na2SO4 NaCl Na2SO4 εo 0.19 0.09 0.12 0.05 0.71 0.50 0.57 0.35
Mo(g/mol) 282.46 169.93 282.46 169.93 ρo(g/m3) 8.95x105 9.94x105 8.95x105 9.94x105
υo 2 2 2 2 819
Table 2.Inferred surface tension for unacidified aerosols from eqns. (3-5), assuming in-particle 820
concentrations of 0.176 or 1.76 Moleate in either 8.6 M NaCl or 10.6 M Na2SO4. 821
822
σ (mN/m) [0.176 M]
σ (mN/m) [1.76 M] Before
Oxidation After
Oxidation (1ppm)
After Oxidation (0.2ppm)
Before Oxidation
After Oxidation
(1ppm)
After Oxidation (0.2ppm)
NaCl 68.1 70.5 71.7 57.5 64.4 68.6 Na2SO4 73.9 74.8 - 63.7 69.9 -
823
Table 3.Inferred surface tension for acidified aerosols from eqns. (3-5), assuming in-particle 824
concentrations of 0.176 or 1.76 M oleate in either 8.6 M NaCl or 10.6 M Na2SO4. 825
826 σ (mN/m) [0.176 M] σ (mN/m) [1.76 M]
Before Oxidation
After Oxidation (1ppm)
Before Oxidation
After Oxidation (1ppm)
NaCl 69.1 72.9 55.5 67.4 Na2SO4 72.4 74.8 66.1 74.8
827 828 829
830
831
832
Figures 833
834
32
835 Figure 1.Experimental setup. The solutions were atomized, and combined with humidified N2; 836
this flow entered the flow tube reactor simultaneously with O3 in an N2 stream. The reactor 837
effluent passed through a drier before being characterized with a Differential Mobility Analyzer 838
(DMA), Condensation Particle Counter (CPC) and a Continuous Flow Streamwise Thermal 839
Gradient CCN Chamber (CFSTGC). 840
33
2
3
4
5
6
789
1C
ritic
al S
S [%
]
3 4 5 6 7 8 9100
Critical Dry Diameter [nm]
0.05 M NaCl0.001 M SO-NaCl0.001 M SO-NaCl-1 ppm O30.001 M SO-NaCl-0.2 ppm O30.01 M SO-NaCl0.01 M SO-NaCl-1ppm O30.01 M SO-NaCl-0.2 ppm O3
0.8
0.7
0.6
0.5
0.4
0.3
0.2
Crit
ical
SS
[%]
65432Wet Diameter [µm]
0.05 M NaCl0.001 M SO-NaCl0.001 M SO-NaCl-1 ppm O30.001 M SO-NaCl-0.2 ppm O30.01 M SO-NaCl0.01 M SO-NaCl-1 ppm O30.01 M SO-NaCl-0.2 ppm O3
A
B
5
6
7
8
9
1
40353025
841
Figure 2.CCN activity of SO/NaCl particles. Particles generated from solutions containing 0.001 842
M or 0.01 M SO mixed with 0.05 M NaCl were exposed to O3 concentrations ranging between 843
0.2-1ppm in an aerosol flow tube reactor. Instrument supersaturation is shown as a function of 844
A) critical dry diameter and B) activated wet diameter. In both plots, the red dots represent the 845
salt calibration, and the red lines are guides to the eye. In panel A) an inset focuses on higher 846
supersaturations. In panel B) the gray lines indicate the standard deviation in the salt calibration. 847
848
34
0.8
0.7
0.6
0.5
0.4
0.3
0.2
Crit
ical
SS
[%]
65432
Wet Diameter [µm]
0.06 M Na2SO40.001 M SO-Na2SO40.001 M SO-Na2SO4-1 ppm O30.01 M SO-Na2SO40.01 M SO-Na2SO4-1 ppm O3
2
3
4
5
6
7
89
1C
ritic
al S
S [%
]
3 4 5 6 7 8 9100
Critical Dry Diameter [nm]
0.06 M Na2SO40.001 M SO-Na2SO40.001 M SO-Na2SO4-1 ppm O30.01 M SO-Na2SO40.01 M SO-Na2SO4-1 ppm O3
A
B
5
6
7
8
9
1
40353025
849
Figure 3.CCN activity of SO/Na2SO4 particles. Particles generated from solutions containing 850
0.001 M or 0.01 M SO mixed with 0.06 M Na2SO4, were oxidized with 1 ppm O3 in an aerosol 851
flow tube reactor. Instrument supersaturation is shown as a function of A) critical dry diameter 852
and B) activated wet diameter. In both plots, the red dots represent the salt calibration, and the 853
red lines are guides to the eye. In panel A) an inset focuses on higher supersaturations. In panel 854
B) the gray lines indicate the standard deviation in the salt calibration. 855
35
0.8
0.7
0.6
0.5
0.4
0.3
0.2
Crit
ical
SS
[%]
65432Wet Diameter [µm]
0.05 M NaCl0.001 M OA-NaCl0.001 M OA-NaCl-1 ppm O30.01 M OA-NaCl0.01 M OA-NaCl-1 ppm O3
2
3
4
5
6
789
1C
ritic
al S
S [%
]
3 4 5 6 7 8 9100
Critical Dry Diameter [nm]
0.05 M NaCl0.001 M OA-NaCl0.001 M OA-NaCl-1 ppm O30.01 M OA-NaCl0.01 M OA-NaCl-1 ppm O3
A
B
5
6
7
8
9
1
40353025
856
Figure 4. CCN activity of SO/NaCl particles exposed to H2SO4. Particles generated from 857
solutions containing 0.001 M or 0.01 M SO mixed with 0.05 M NaCl were oxidized with 1 ppm 858
O3 in a flow tube reactor. Instrument supersaturation is shown as a function of A) critical dry 859
diameter and B) activated wet diameter. In both plots, the red dots represent the salt calibration, 860
and the red lines are guides to the eye.In panel A) an inset focuses on higher supersaturations. In 861
panel B) the gray lines indicate the standard deviation in the salt calibration. 862
863
36
2
3
4
5
6
7
89
1C
ritic
al S
S [%
]
3 4 5 6 7 8 9100
Critical Dry Diameter [nm]
0.06 M Na2SO40.001 M OA-Na2SO40.001 M OA-Na2SO4-1 ppm O30.01 M OA-Na2SO40.01 M OA-Na2SO4-1 ppm O3
0.8
0.7
0.6
0.5
0.4
0.3
0.2
Crit
ical
SS
[%]
65432Wet Diameter [µm]
0.06 M Na2SO40.001 M OA-Na2SO40.001 M OA-Na2SO4-1 ppm O30.01 M OA-Na2SO40.01 M OA-Na2SO4-1 ppm O3
A
B
5
6
7
8
9
1
403530
864
Figure 5. CCN activity of SO/Na2SO4 particles exposed to H2SO4. Particles generated from 865
solutions containing 0.001 M or 0.01 M SO mixed with 0.06 M Na2SO4, were oxidized with 1 866
ppm O3 in an aerosol flow tube reactor. Instrument supersaturation is shown as a function of A) 867
critical dry diameter and B) activated wet diameter. In both plots, the red dots represent the salt 868
calibration, and the red lines are guides to the eye. In panel A) an inset focuses on higher 869
supersaturations. In panel B) the gray lines indicate the standard deviation in the salt calibration. 870
871